Canonical Allele Identifier: PA2825280022
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2417599
ClinVar RCV Id: RCV003115068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Met962Ile
CA388026273
NM_001005918.3:c.2886G>T
CA388026276
NM_001005918.3:c.2886G>C
CA388026279
NM_001005918.3:c.2886G>A